Canonical Allele Identifier: CA798018767

Gene: DCK

Linked Data

• dbSNP Id: rs1428833577
• gnomAD v3: 4-71030695-A-C
• gnomAD v4: 4-71030695-A-C
• MyVariant Identifiers: chr4:g.71896412A>C (hg19) ; chr4:g.71030695A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71030695A>C , CM000666.2:g.71030695A>C	GRCh38
NC_000004.11:g.71896412A>C , CM000666.1:g.71896412A>C	GRCh37
NC_000004.10:g.72115276A>C	NCBI36
NG_023303.1:g.42148A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286648.10:c.*1317A>C MANE Select	ENSP00000286648.5:n.*1317A>C
ENST00000286648.9:c.*1317A>C	ENSP00000286648.5:n.*1317A>C
ENST00000503359.5:c.*2044A>C	ENSP00000426389.1:n.*2044A>C
ENST00000504730.5:c.*1384A>C	ENSP00000425578.1:n.*1384A>C
ENST00000504952.1:c.*1243A>C	ENSP00000421508.1:n.*1243A>C
NM_000788.2:c.*1317A>C	NP_000779.1:n.*1317A>C
NM_000788.3:c.*1317A>C MANE Select	NP_000779.1:n.*1317A>C